Adair Breast Clamp

GUDID 00192896102644

Adair Breast Clamp

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable
Primary Device ID00192896102644
NIH Device Record Keyfc4f9c1e-fe90-41f0-ab83-75bfe61d0e6a
Commercial Distribution StatusIn Commercial Distribution
Brand NameAdair Breast Clamp
Version Model Number140-407
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896102644 [Primary]
GS100192896102644 [Primary]
GS100192896102644 [Primary]
GS100192896102644 [Primary]
GS100192896102644 [Primary]
GS100192896102644 [Primary]
GS100192896102644 [Primary]
GS100192896102644 [Primary]
GS100192896102644 [Primary]
GS100192896102644 [Primary]
GS100192896102644 [Primary]
GS100192896102644 [Primary]
GS100192896102644 [Primary]
GS100192896102644 [Primary]
GS100192896102644 [Primary]

FDA Product Code

GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY
GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY
GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY
GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY
GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY
GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY
GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY
GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY
GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY
GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY
GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY
GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY
GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY
GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY
GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896102644]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102644]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102644]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102644]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102644]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102644]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102644]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102644]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102644]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102644]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102644]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102644]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102644]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102644]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102644]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-06-23
Device Publish Date2020-06-15

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